单倍率不足
生物
核仁
抄写(语言学)
RNA聚合酶Ⅰ
遗传学
RNA聚合酶Ⅱ
特雷彻-柯林斯综合征
RNA聚合酶Ⅲ
突变体
基因
RNA聚合酶
核糖核酸
颅面
发起人
基因表达
表型
哲学
语言学
细胞质
作者
Chen-I Lin,Ning-Hsing Yeh
标识
DOI:10.1016/j.bbrc.2009.06.050
摘要
Mutations in treacle lead to Treacher Collins syndrome (TCS), an autosomal dominant disorder of craniofacial development. Treacle associates with upstream binding factor (UBF) to regulate rRNA gene (rDNA) transcription, but the precise mechanisms mediated by treacle remain elusive. Here we show that the central repeated domain of treacle binds with RNA polymerase I (Pol I), while that the treacle C-terminus is involved in rDNA promoter recognition and UBF recruitment. Knockdown of treacle resulted in dispersion of Pol I and UBF away from nucleolus, whereas interactions of treacle with Pol I and rDNA promoter were not disrupted by UBF depletion. These findings indicate that treacle, but not UBF, is essential for nucleolar recruitment of Pol I transcription complex. Furthermore, C-terminally truncated treacle, mimicking TCS-associated mutations, failed to target to the nucleolus, possibly causing loss-of-function in the mutant treacle. Our observations support that TCS results from haploinsufficiency of treacle.
科研通智能强力驱动
Strongly Powered by AbleSci AI